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Proteomic analysis of Haloferax volcanii reveals salinity-mediated regulation of the stress response protein PspA

机译:Haloferax Volcanii的蛋白质组学分析显示出盐度介导的应力反应蛋白PSPA的调节

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A proteomic survey of the halophilic archaeon Haloferax volcanii was performed by comparative two-dimensional gel electrophoresis in order to determine the molecular effects of salt stress on the organism. Cells were grown under optimal (2.1?M) and high (3.5?M) NaCl conditions. From this analysis, over 44 protein spots responsive to these conditions were detected. These spots were excised, digested in-gel with trypsin, subjected to QSTAR tandem mass spectrometry (LC/MS/MS) analysis, and identified by comparing the MS/MS-derived peptide sequence to that deduced from the H. volcanii genome. Approximately 40?% of the proteins detected (18 in total) displayed differential abundance based on the detection of at least two peptide fragments per protein and overall MOWSE scores of ≥75 per protein. All of these identified proteins were either uniquely present or 2.3- to 26-fold higher in abundance under one condition compared to the other. The majority of proteins identified in this study were preferentially displayed under optimal salinity and primarily involved in translation, transport and metabolism. However, one protein of interest whose transcript levels were confirmed in these studies to be upregulated under high salt conditions was identified as a homologue of the phage shock protein PspA. The pspA gene belongs to the psp stress-responsive regulon commonly found among Gram-negative bacteria where its transcription is stimulated by a wide variety of stressors, including heat shock, osmotic shock and prolonged stationary-phase incubation. Homologues of PspA are also found among the genomes of cyanobacteria, higher plants and other Archaea, suggesting that this protein may retain some aspects of functional conservation across the three domains of life. Given its integral role in sensing a variety of membrane stressors in bacteria, these results suggest that PspA may play an important role in hypersaline adaptation in H. volcanii.
机译:通过对比二维凝胶电泳进行嗜盐古仑Haloferax Volcanii的蛋白质组学调查,以确定盐胁迫对生物体的分子效果。细胞在最佳(2.1·m)和高(3.5μm)NaCl条件下生长。从该分析中,检测到响应于这些病症的44种蛋白质点。切除这些斑点,用胰蛋白酶消化凝胶中的凝胶,经受QSTAR串联质谱(LC / MS / MS)分析,并通过将MS / MS衍生的肽序列与从H- volcanii基因组推导的胰蛋白酶进行鉴定。基于检测到每种蛋白质的至少两种肽片段和每种蛋白质的总分数≥75的总分数检测到约40℃的蛋白质(总共18个)显示差异丰度。与另一个条件相比,所有这些鉴定的蛋白质在一个条件下唯一存在或在丰度下较高。本研究中鉴定的大多数蛋白质优先展示在最佳盐度下,主要参与翻译,运输和代谢。然而,在这些研究中证实了转录物水平的一种蛋白质,以在高盐条件下上调作为噬菌体休克蛋白PSPA的同源物。 PSPA基因属于PSP应激响应性调节件,常见于革兰氏阴性细菌中,其转录受各种压力源刺激,包括热休克,渗透休克和长期固定相孵化。 Cyanobacteria,高等植物和其他古亚群体的基因组也发现了PSPA的同源物,这表明该蛋白质可以保留在生命的三个域中的功能保护的一些方面。鉴于其在感测细菌中的各种膜压力源方面的积分作用,这些结果表明PSPA可能在H. Volcanii中的Hypersaline适应中发挥重要作用。

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